W11G (p.Trp11Gly) variant of SLC18A2 (Q05940)
W11G (p.Trp11Gly) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
W11G (p.Trp11Gly) variant details
- p.Trp11Gly
- ExAC rs745855361
- gnomAD rs745855361
- Missense
- Variant Prioritization Score for Impact Estimate 0.255
- CADD 24.70
- PolyPhen-2 0.53
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available